Colon Cancer: Gene >> ENDOU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47713377:47713377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763T>A
AA Mutation	p.Ser255Thr(p.S255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47710870:47710870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165T>C
AA Mutation	p.Trp389Arg(p.W389R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47725365:47725365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49T>A
AA Mutation	p.Trp17Arg(p.W17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47717003:47717003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438G>T
AA Mutation	p.Glu146Asp(p.E146D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47718147:47718147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47713385:47713385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748452815
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000422538
Start	47712593:47712593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895T>C
AA Mutation	p.Phe299Leu(p.F299L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422538
Start	47713327:47713327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000422538
Start	47716889:47716889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150299683
CDS Mutation	c.551+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ENDOU

No Mutation Annotation!